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Everolimus in Combination With Exemestane in the Treatment of Postmenopausal Women With Estrogen Receptor Positive Locally Advanced or Metastatic Breast Cancer Who Are Refractory to Letrozole or Anastrozole
Not Recruiting
Trial ID: NCT00863655
Purpose
There are no treatments specifically approved after recurrence or progression on a non
steroidal aromatase inhibitors (NSAI). In light of the need for new treatment options for
postmenopausal women after failure of prior NSAI therapy, the purpose of this Phase III study
is to compare efficacy and safety of a treatment with exemestane + everolimus to exemestane +
placebo in postmenopausal women with estrogen receptor positive locally advanced or
metastatic breast cancer refractory to NSAI.
Official Title
A Randomized Double-Blind, Placebo-Controlled Study of Everolimus in Combination With Exemestane in the Treatment of Postmenopausal Women With Estrogen Receptor Positive Locally Advanced or Metastatic Breast Cancer Who Are Refractory to Letrozole or Anastrozole
Stanford Investigator(s)
Allison W. Kurian, M.D., M.Sc.
Professor of Medicine (Oncology) and of Epidemiology and Population Health
Eligibility
Inclusion Criteria:
- Adult women (≥ 18 years of age) with metastatic or locally advanced breast cancer not
amenable to curative treatment by surgery or radiotherapy.
- Histological or cytological confirmation of estrogen-receptor positive (ER+) breast
cancer
- Postmenopausal women.
- Disease refractory to non steroidal aromatase inhibitors (NSAI),
- Radiological or clinical evidence of recurrence or progression on or after the last
systemic therapy prior to randomization.
- Patients must have at least one lesion that can be accurately measured or bone lesions
in the absence of measurable disease as defined above.
Exclusion Criteria:
- HER2-overexpressing patients
- Patients with only non-measurable lesions other than bone metastasis (e.g. pleural
effusion, ascites etc.).
- Patients who received more than one chemotherapy line for Advanced Breast Cancer.
- Previous treatment with exemestane or mTOR inhibitors.
- Known hypersensitivity to mTOR inhibitors, e.g. sirolimus (rapamycin).
- Radiotherapy within four weeks prior to randomization
- Currently receiving hormone replacement therapy,
Other protocol-defined inclusion/exclusion criteria may apply
Intervention(s):
drug: Everolimus
drug: Exemestane
drug: Everolimus Placebo
Not Recruiting
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305
Cancer Clinical Trials Office
650-498-7061